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期刊名:Egyptian journal of medical human genetics

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ISSN:1110-8630

e-ISSN:2090-2441

IF/分区:1.1/Q4

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共收录本刊相关文章索引47
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Ehtisham Ul Haq,Asma Naeem,Usman Ayub Awan et al. Ehtisham Ul Haq et al.
Background: β-thalassemia is a common autosomal recessive blood disorder caused by mutations in the β-globin gene, with highly variable carrier frequencies across different regions. In Pakistan, cultural practices such ...
Nataliia Karpova,Olga Dmitrenko,Ekaterina Arshinova et al. Nataliia Karpova et al.
Background: Iron deficiency is a cause of anemia in pregnant women. Iron metabolism is closely related to zinc levels and the state of zinc-containing proteins. Zinc-binding proteins (ZNFs) can also bind other metal ions....
Estela Morales Peralta,Yaíma Zúñiga Rosales,Teresa Collazo Mesa et al. Estela Morales Peralta et al.
Purpose: To determine the relationship between the genotypes of the TaqI polymorphism of VDR gene and the clinical forms of COVID-19 in Cuban patients. Me...
Ali H Ad&#x;hiah,Noor T Al-Bayatee,Aeshah A Ahmed Ali H Ad&#x;hiah
A cross-sectional observational study was conducted on 213 patients with COVID-19 who did not have a clinical history of diabetes at hospital admission. One week after hospitalization, they were stratified by random blood glucose levels. It...
Olanrewaju Ayodeji Durojaye,Nkwachukwu Oziamara Okoro,Arome Solomon Odiba Olanrewaju Ayodeji Durojaye
Background: The novel coronavirus SARS-CoV-2 is currently a global threat to health and economies. Therapeutics and vaccines are in rapid development; however, none of these therapeutics are considered as absolute cure, a...
Asal Gailan Abdul-Qadir,Bassam Musa Al-Musawi,Rabab Farhan Thejeal et al. Asal Gailan Abdul-Qadir et al.
Background: Cystic fibrosis (CF) is an autosomal recessive multisystem disease that results from mutation(s) of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. More than 2100 mutations and polymorphis...
Khyber Saify,Mohammad Sarwar Alborz,Mostafa Saadat Khyber Saify
Background: There are preliminary studies about the association between COVID-19 and ABO phenotypes and the results are controversial. There are only two studies which investigated the association of Rh blood groups in ad...
Ali H Ad&#x;hiah,Maha H Abdullah,Mustafa Y Alsudani et al. Ali H Ad&#x;hiah et al.
Background: A case-control study was performed to examine age, gender, and ABO blood groups in 1014 Iraqi hospitalized cases with Coronavirus disease 2019 (COVID-19) and 901 blood donors (control group). The infection was...
Mayank Chaudhary Mayank Chaudhary
Background: Angiotensin-converting enzyme 2 (ACE2) is a metallopeptidase that primarily functions as a negative regulator of renin angiotensin system (RAS) by converting angiotensin II (Ang II) to angiotensin 1-7. Contrar...
Babayemi Olawale Oladejo,Covenant Femi Adeboboye,Tinuola Tokunbo Adebolu Babayemi Olawale Oladejo
Background: Numerous research studies have identified specific human gene variants that affect enhanced susceptibility to viral infections. More recently is the current pandemic where the SARS-CoV-2 infection has shown a ...